ZITHROMAX Detail

Drug Name(s):
ZITHROMAX

FDA Application No.:
NDA 050693

Active Ingredient(s):
AZITHROMYCIN

Company:
PFIZER

Original Approval or Tentative Approval Date:
November 21, 1999

Products on Application NDA 050693:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AZITHROMYCIN	EQ 1GM BASE/PACKET	FOR SUSPENSION; ORAL	Prescription	none

Recall Notices

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FDA Announces Class I Recall of Ophthalmic Surgical Device
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KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

ZITHROMAX Detail

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